Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1969, 34, 3801-3810
https://doi.org/10.1135/cccc19693801

Neurotropic and psychotropic substances. XXXVIII. Derivatives of 10,11-dihydrodibenzo[b,f]selenepin

K. Šindelář, J. Metyšová and M. Protiva

Crossref Cited-by Linking

  • Okba Aissam, Simón Marqués Pablo, Matsuo Kyohei, Aratani Naoki, Yamada Hiroko, Rapenne Gwénaël, Kammerer Claire: Synthesis of π-conjugated polycyclic compounds by late-stage extrusion of chalcogen fragments. Beilstein J. Org. Chem. 2024, 20, 287. <https://doi.org/10.3762/bjoc.20.30>
  • Hori Hideaki, Yamazaki Shoko, Yamamoto Kagetoshi, Murata Ichiro: Ein monocyclisches Selenepin: Synthese und Charakterisierung von 2,7‐Di‐tert‐butyl‐4,5‐selenepindicarbonsäurediethylester. Angewandte Chemie 1990, 102, 450. <https://doi.org/10.1002/ange.19901020436>
  • Hori Hideaki, Yamazaki Shoko, Yamamoto Kagetoshi, Murata Ichiro: A Monocyclic Selenepine: Synthesis and Characterization of Diethyl 2,7‐Di‐tert‐butyl‐4,5‐selenepinedicarboxylate. Angew. Chem. Int. Ed. Engl. 1990, 29, 424. <https://doi.org/10.1002/anie.199004241>
  • Scarborough Robert M., Smith Amos B.: An efficient general synthesis of ω-olefinic methyl esters. Tetrahedron Letters 1977, 18, 4361. <https://doi.org/10.1016/S0040-4039(01)83508-5>
  • Liotta Dennis, Santiesteban Hector: Nucleophilic ring opening of lactones via SN2-type reaction with uncomplexed phenyl selenide anion. Tetrahedron Letters 1977, 18, 4369. <https://doi.org/10.1016/S0040-4039(01)83510-3>
  • SINDELAR K., METYSOVA J., PROTIVA M.: ChemInform Abstract: NEUROTROPE UND PSYCHOTROPE SUBSTANZEN 38. MITT. DERIVATE VON 10,11‐DIHYDRO‐DIBENZO(B,F)SELENEPIN. Chemischer Informationsdienst. Organische Chemie 1970, 1. <https://doi.org/10.1002/chin.197011300>